Waiting Child Photolistings – Boys & Girls Need Families

Brian is 10 years old
Olivia is 13 years old
Victor is 12 years old
Tyler is 11 years old

Married couples only

No age requirements

No limit to amount of children already in the home

Timeline: 4-8 months from start of homestudy to travel

Travel: Only one parent needs to travel. One long trip lasting 30-35 days or it can be broken up into two shorter trips, each lasting 10-12 days.

Costs vary be region. This is a special needs adoption, so reduced agency fee and foreign fee. The agency can help you apply for grants and receive donations toward the adoption fund.

Please contact Victoria Tucker  at Good Hope Adoption Services: vtuckergoodhope@gmail.com

*This post has been updated. ‘Violet’ and ‘Alice’ now have committed adoptive families

10 Children with HIV Need Parents

RainbowKids newsletter dated February 7, 2012 is reporting about 10 children with HIV in need of adoptive parents. All of the children are listed with the very reputable agency CHSFS. Contact intchild@chsfs.org about these little ones:

  • Girl in Eastern Europe born 10/2007
  • Boy in Eastern Europe born 7/2009
  • Boy in Eastern Europe born 7/2008
  • Boy in Asia born 3/2004
  • Boy in Latin America born 11/2008
  • Girl in Latin America born 11/2004
  • Boy in Latin America born 6/2009
  • Boy in Latin America born 10/2003
  • Boy in Latin America born 5/2003
  • Boy in Africa born 3/2007

Pretty and Smart Girl Needs a Family ~ Waiting Child Photolisting

“Hope”  was born in November 2005. She has dark eyes and she is an amazing little girl. She gets along well with other children. She is very smart. When an adult explains something to her, she listens carefully and makes her findings. When she is interested in something, she asks questions. She is inquisitive, curious and communicative. She is also described as being charming and affectionate. This child really needs a loving family. It is believed that whatever developmental delays she may have from institutional life can be overcome. She is a cheerful girl and she likes helping take care of the younger children. She is a truly beautiful girl.  She was transferred to the older child orphanage toward the end of 2008. She is so gentle and waits patiently for someone to show her attention or affection. She has a confirmed HIV-positive diagnosis. The chances of a child this age with HIV being adopted by a local family in this particular region are almost zero. The most recent photos were taken in summer 2009.

Waiting Children in China

There are occasionally children in China with HIV who are in need of international adoptive families. The placing agencies who have advocated for orphans with HIV in China include Adoption Advocates International, Lifeline, Wasatch and Great Wall. Exceptions  can sometimes be made to China’s eligibility requirements when adopting a child with HIV.

Life Expectancy for People Living with HIV/AIDS

It’s hard to find recent scientific and clinical studies about life expectancy of people living with HIV/AIDS in the western world. Keep in mind that life expectancy varies so much depending on when a person is diagnosed, how diligent the patient is with medication compliance, as well as their social situation (nutrition, street life, drug use, accessing medical care, mental illness, prostitution, co-infections, etc). This recent report in Medical News Today is indicating an average life expectancy of 65.8 years in the United Kingdom.

International Adoption from BURUNDI

Lutheran Social Service of MN has a pilot adoption program for Burundi. The agency has indicated that HIV+ children are in need of families. Married couples must be married 5 years. Single females age 30-55 can adopt. There is no restriction to the number of children in the home. Parents must not have any major medical conditions or criminal background. Total travel is 3-4 weeks.

All Grown Up With HIV

The current edition of POZ magazine has an article titled “All Grown Up with HIV”. It features 4 individuals who were infected with HIV as youth. Two were infected perinatally and two were infected behaviorally as teenagers. I’m featuring the 2 individuals who were infected perinatally as that is the topic of this blog. 

Thirty years into the epidemic, a new crop of kids faces adulthood—with HIV. From babies born with the virus to teens who acquired it behaviorally, members of this new generation struggle to navigate survival while making their way through the world. The stories of these four brave young people are examples for how to succeed in spite of HIV. They also serve as cautionary tales, reminding us of the price we pay for not teaching our children well. Let lessons be learned.

Lafayette Sanders, 24, West Philadelphia, 
Perinatally Infected
Having found power in disclosure and self-advocacy, musician Lafayette has found a new life. Now that he has broken down his own stereotypes about HIV, Lafayette is trying to help other people do the same.

I was in the doctor’s office. I was 13; it was a few months after my mother passed away. My grandmother took me for a checkup, and I was then told about me being HIV positive. My grandmother knew what I didn’t: My mom died of HIV, HIV that she passed along to me. They told me, and I took the meds but didn’t learn anything about HIV. At that age, I had no idea about the stigma or life spans. Having to take medications was like taking vitamins: You don’t know what it’s for, you just do it ’cause it’s good for you.

And then high school hit. I started to hang around kids my age, and everybody was talking about sex, and HIV came up in the picture. I wanted to tell them I was positive, but I didn’t know that much about it to tell and to be able to defend myself. I didn’t want to be looked at as different. So I didn’t disclose. There were so many feelings, and I was so angry for so long. It took me a long time to get over the anger at my mom—that she didn’t tell me herself, when we were so close and shared everything, and then to find out this big thing and to deal with it on my own. I was angry at her, God, myself, everybody. And then there was my grandmother. My grandmother was the primary guardian to my sister and me after my mother passed. My sister, who is not HIV positive, was too young to remember my mother’s death. My grandmother, who is a sweet and caring woman but also very traditional, put me in a box of fear. She made me believe that disclosing my status would change how people treated me, how they looked at me. It wasn’t true, to me—I knew someday people would understand and accept me for me.

When I was maybe 17 or 18, I woke up every day thinking about HIV and [I wanted to make it go away, to pretend it wasn’t there] so I stopped taking medication. I would hide it, pretend. I was young and irresponsible. And I was having sex.

The turning point came with my last two girlfriends. I disclosed to [the first one] right off the bat. Still we were reckless and irresponsible, and she got pregnant. She had a miscarriage, and to this day she’s negative. Second relationship, almost the same thing. She had an abortion. I was sitting in an abortion clinic, and I thought, “How the hell did I end up here? I’m reckless, and the people I’m with are reckless.” That was my wake-up call, the moment of “You have to get your shit together.”

I hooked up with iChoose2live [a youth organization designed to encourage self-esteem and awareness about HIV and other issues]. I thank God for everyone He has placed in and out of my life. He uses who He chooses when He chooses. If it weren’t for me meeting [hip-hop artist] Lee Mekhai at a show in Philly, I wouldn’t have found out about iChoose2live and the founder Shenille Melton. That opened a lot of doors for me as far as reaching the youth.

Since I had already taken a course for certification in HIV Peer Education through Philadelphia FIGHT’s program, Project TEACH, I thought about disclosing my status. For 10 years, my grandmother was the voice discouraging me from disclosing. I was secluded. She drilled into me that disclosing was not safe, that “the neighbors are gonna look at you this way, no one is gonna look at you the same way or accept you.” But as I began to educate myself about the virus, how it works and what it does, I began to lose the fear of disclosing. Then after I linked up with iChoose2live, I came out in a big way through interviews and the work [I did with that group].

My grandmother kicked me out when I told her I would be doing an open interview about me being positive with The Philadelphia Inquirer, which [was published] on September 13, 2010. [At that time,] I had no job, no money, I was struggling. But a lot of positive things came from my disclosure. People emailed me to thank me for being honest about my HIV status. I was intrigued and blessed that my story could help others. I started speaking to groups at the children’s hospital. Kids looked up to me.

I’ve learned that kids in public schools aren’t being taught what they really need to know. HIV is that disease that’s swept under the rug; no one talks about it. And youth are spreading [the virus] because they’re uneducated, misinformed and not being reached out to enough. I honestly think there should be mandatory classes in all middle schools through college for educating about HIV/AIDS [and other sexually transmitted infections].

Positive people my age need to be out there. You can’t have a 48-year-old man talking to kids about this. No one listens. You need someone like me, someone who is living with [HIV]—then it becomes more real. It’s a great feeling to be able to do that. And that’s just me! One person. Imagine if everyone was doing it, if everyone got together. We may not be able to stop this pandemic, but we can inform, educate and empower, and we can slow down the rates of HIV transmission.

I would like to write a book about my life living with HIV and just my life in general. I know my story and experiences within these past 24 years can help educate, empower and change other people’s lives—people of all ages. My story will heal lives all over and most importantly let everyone know the power of God. He’s the only reason why I’m still alive and healthy.

I’m looking forward to the future, staying healthy and changing people’s lives.

Paige Rawl, 17, Indianapolis, Perinatally Infected
She is a high school student, an athlete, a teen. Having encountered and overcome enormous stigma, Paige has flourished—making a place for herself in a world that hasn’t figured out how to make a place for youth living life with HIV.

My name is Paige, and I’ve been positive for 17 years. My mom unknowingly passed it on to me, and she found out her status right before I turned 3. She contracted the disease from my father—we’re not sure how or when he contracted HIV. That’s just the way it goes.

My mom told me I was positive when I was in fifth grade. But I didn’t get it. I took the pills because that’s what you do when you’re young and your mom gives you pills. And then middle school happened.

In sixth grade I confided in my best friend; I told her I’d been HIV positive since birth. Within two weeks, she had told her sister and other people, and they told others, and eventually the whole school knew. Everyone. People threatened to beat me up; they left a note on my locker saying “No AIDS at [school name].” They gave me a nickname: “PAIDS.” They told each other not to drink after me, as if HIV was contagious [that way]. I went from [being] popular to having no friends.

In eighth grade, I made the soccer team. I was going to be part of a team. Then someone told my coach I had AIDS. At our first away game, my coach approached me on the bench, in front of other players, and asked, “By the way, I heard that you have AIDS. Is that true?” I said no, because I don’t have AIDS, I am HIV positive and there is a difference.

I was so upset. This was a coach. Someone who should know. I told mom, who confronted my coach at school. She admitted to asking me and went on to say, “The soccer team could use my HIV status to an advantage, and the other team will be afraid, and I can score goals.” I withdrew from the school and finished out my year with homeschooling.

My mother has been so supportive. And my family. I didn’t have to disclose to them; my mom told them before she even told me. But you need support of different kinds. Since the bullying, the coach, the discrimination, I’ve started seeing a counselor and started taking an antidepressant. It’s OK to look for help, and it’s OK to get help.

I realized that I can help other people too. I wanted to take a bad situation and turn it into something good by helping others know about HIV and the precautions they should take. So I became a peer sex educator and a certified HIV/AIDS educator through the American Red Cross.

I also started looking for support groups and even tried to start one. I searched the Internet, I asked questions, and I was referred to Camp Kindle [a free summer camp for kids living with or affected by the virus]. Meeting other kids [like me] has given me people to talk to, people who can relate to what I’m going through.

These days, I am open about my status to everyone. I take the time to speak to my peers, raise awareness and share my story. Funny, after disclosing to my former best friend in sixth grade and it spreading through the school, it just became easier to tell people who didn’t already know. For the most part, there’s a positive response. The fear that I should not have disclosed my status so soon just doesn’t exist anymore.

I know firsthand that there are still big misconceptions out there about how you can and cannot contract HIV. [We need] more education among youth in the U.S., and there should be more support groups. Youth need to see themselves reflected in what’s taught, in the information they are given.

The hardest part about living with HIV is the stigma that goes along with it. But I have hope. Two years ago, I was the freshman class president, on the JV cheerleading squad and on the soccer team. Last year, I was part of the student government and on the varsity squad. I volunteer, I share my story, I travel. I have hope.

Adoption Photolistings including Older Children

Wow! Look at those stunning blue eyes. Jack is a good boy. He was born in 2001. He would like to be adopted. He is HIV-positive and doing well physically and developmentally. Married couples may inquire.
Don’t mind the pink shirt, Brance is a boy! He is 5 years old and was born testing positive for HIV and HepC. Married couples who can travel can inquire.
Autumn is a very pretty girl who is active, sweet and sociable. She is healthy and participates in life fully and is developing normally. She was born with HIV and receives the appropriate medications. Married couples ages 25-64 years with health insurance may apply to adopt her.
Hadley is a reserved and sweet young lady. She is a healthy normal 9 year old girl with long silky blond hair and light hazel eyes. She is tall for her age. She is developing normally and is at a location with excellent care. She is noted as being VERY patient, reserved, considerate and kind, great kid. She might have a brother, this can be verified upon inquiry. She was born HIV positive. Married couples who can travel should inquire.
Cole is a cute little stinker! He is all boy Little Cole has dirty blond hair and huge brown eyes. He is ready to hit school, run around the house in Buzz Lightyear pajamas and race hot wheels. This healthy chunky little boy has no developmental delays. He is HIV positive. He is doing well and he is a healthy, active little boy. He can be adopted quickly by a married couple with one parent age 51 or younger.
Val is a 12 year old boy with HIV and normal development. Married couples with one parent within 45 years of the age of this child may apply.
Collin is a 12 year old boy with HIV. He is developing normally. Adoptive parents should be no more than 45 years older than Collin.
Paige has such soulful eyes and stunning blond hair. She was born in 1997 and longs for a family. She was born HIV positive but is doing very well physically. She would like to be adopted into a happy family! Married couples may inquire.
Isaac is a lively young man born in 1997. He has a pigeon chest, is HIV positive and there is a note in his medical records about his tonsils-possibly they need to be removed. He is active, friendly and does well in school. His physical issues do not cause him any problems. He would like to be adopted, married couples may inquire.
Eden is a precious young girl waiting to be adopted. Despite being born with both HIV and Hep C, she is doing rather well. She is doing well physically at this time but would love a family to do all those girl things! Married couples may inquire.
Charlotte has blond hair and brown eyes and she was born in 1997. She longs to be adopted. This sweet little teen girl was born HIV positive and has a mild astigmatism, but is generally physically healthy. Married couples may inquire.

These children were on the photolisting website http://waitingchildren.wordpress.com/ .  Email me if you need contact info. 

New Guidelines for Treatment of HIV-positive Children

The United States Department of Health and Human Services (HHS) has released an updated version of its “Guidelines for the Use of Antiretroviral Agents in Pediatric HIV Infection.”

The guidelines contain updated recommendations in several areas, including when to start antiretroviral therapy and factors to consider in selecting an antiretroviral regimen. The guidelines also contain new sections on rates and management of various side effects related to the use of antiretrovirals.

The guidelines are intended for use by doctors and other health care professionals when treating HIV-positive children and teens. They were last updated in August 2010.

Key updates to various sections of the guidelines are summarized below.

Start Of Antiretroviral Therapy

Suggestions for when to initiate antiretroviral therapy vary according to age group.

Antiretroviral therapy is now recommended for children five years or older who have CD4 (white blood cell) counts of less than 500 cells per microliter, even if their symptoms are mild or nonexistent. Previous guidelines recommended treatment at a CD4 count threshold of 350 cells per microliter.

The guidelines continue to recommend treatment for children aged one year or older who have normal CD4 counts but HIV viral loads (amount of HIV in the blood) of 100,000 copies per milliliter of blood or higher, regardless of whether or not they have symptoms.

For children under the age of 12 months, the guidelines also continue to recommend starting antiretroviral therapy regardless of CD4 count, viral load, or the presence or absence of symptoms. Several studies have shown that starting therapy early in children of this age significantly reduces the chances a child will progress to AIDS or die.

In children with normal CD4 counts whose HIV viral loads are less than 100,000 copies per milliliter and who have mild or no symptoms initiation of treatment can be either considered or deferred.

Selection Of Antiretroviral Regimens

As with adults, all HIV-positive children should be treated using combination therapy that includes at least three different antiretroviral drugs from two different classes.

For children aged 14 days to three years, the preferred initial treatment regimen is now Kaletra(lopinavir/ritonavir) plus two nucleoside reverse transcriptase inhibitors (NRTIs). Viramune (nevirapine)-based regimens are now considered an alternative regimen in this age group.

However, due to recent information on toxicity of Kaletra in newborn infants, particularly premature infants, Kaletra should not be given to newborns until at least 42 weeks from the date of the mother’s last menstrual period and 14 days after birth (see related AIDS Beacon news).

For children older than six years, Reyataz (atazanavir) boosted with low-dose Norvir (ritonavir) has been added as a second preferred protease inhibitor for initial treatment regimens; Kaletra is already considered a preferred protease inhibitor for this age group.

The preferred dual-NRTI regimen backbones for initial therapy in children are zidovudine (Retrovir) plusEpivir (lamivudine) or Emtriva (emtricitabine) (any age), Ziagen (abacavir) plus Epivir or Emtriva (children three months or older), and Viread (tenofovir) plus Epivir or Emtriva (children 12 years or older who have finished puberty).

Two new alternate dual-NRTI backbones have been added to the guidelines: didanosine (Videx) plus Epivir or Emtriva (any age), and Viread plus Epivir or Emtriva (children 12 years or older in intermediate stages of puberty). Viread plus Epivir or Emtriva is now listed as a possibility under special circumstances for children 12 years or older in the initial stages of puberty.

The guidelines do not recommend use of the new antiretroviral Edurant (rilpivirine) in children for initial antiretroviral regimens due to lack of information on dosages for children and the absence of a child-friendly formulation of the drug.

The guide continues to recommend that patients who have never received antiretroviral therapy complete antiretroviral drug resistance testing before choosing which drugs to use for treatment.

Monitoring Of HIV-Positive Children

The updated guidelines now note that transient viral load increases of up to 1,000 copies per milliliter (“blips”) are normal and should not be considered a sign of treatment failure.

The guide also recommends that urinalysis be conducted in children at their first visit and repeated every six to 12 months. Urinalysis usually measures aspects of a person’s urine such as pH, presence or absence of blood or protein, and signs of a possible bacterial infection.

To read the article in it’s entirety, click here